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    Brand: Septodont

    Septodont Septanest® SP Articaine hydrochloride 4% and Epi 1:100,000 Inj, 50x1.7ml Carp/Bx

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    Septanest contains Articaine HCI 4% with 1:100,000 epinephrine injection. Septanest is indicated for local, infiltrative, or conductive anesthesia in both simple and complex dental procedures. Septanest with epinephrine 1:100,000 is preferred during operative or surgical procedures when improved visualization of the surgical field is desirable.

    Indications:

    • Local or loco-regional dental anesthesia in patients of at least 4 years old

    Key Features:

    • Fast onset to avoid delay before effective analgesia is achieved
    • No-methylparaben formulation to avoid allergic reactions on sensitive patients
    • Latex-free plungers and seals
    • High epinephrine concentration to improve blood control on the procedure’s site
    • Terminal sterilization of product/cartridges for safe use
    • Milar label covered glass cartridges to minimize risk of wound in the event of a cartridge breakage

    Presentation:

    • Box containing 5 blisters of 10 x 1.7ml glass cartridges

    Risk:

    • Septanest® SP is indicated for local, infiltrative, or conductive anesthesia in both simple and complex dental procedures. Septanest® SP with epinephrine 1:100,000 is preferred during operative or surgical procedures when improved visualization of the surgical field is desirable. Reactions to Septanest® SP (pain and headache, for example, or convulsions or respiratory arrest following accidental intravascular injection) are characteristic of those associated with other amide-type local anesthetics. Septanest® SP contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. Accidental intravascular injection may be associated with convulsions, followed by central nervous system or cardiorespiratory depression and coma, progressing ultimately to respiratory arrest. Dental practitioners and/or clinicians who employ local anesthetic agents should be well versed in diagnosis and management of emergencies that may arise from their use. Resuscitative equipment, oxygen, and other resuscitative drugs should be available for immediate use. Septanest® SP, along with other local anesthetics, is capable of producing methemoglobinemia. The clinical signs of methemoglobinemia are cyanosis of the nail beds and lips, fatigue and weakness. If methemoglobinemia does not respond to administration of oxygen, administration of methylene blue intravenously 1-2 mg/kg body weight over a 5 minute period is recommended. Please see the Package Insert for prescribing information.

    Package contains:

    • 50 cartridges – A box of 5 blisters of 10 x 1.7 ml glass cartridges
    Part number: 211299145
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    Geistlich Bio-Oss® 0.25-1mm, 0.5g=1cc, 1 Vial/Bx

    Geistlich Bio-Oss® is a sterile, biocompatible porous bone mineral substitute, which is physically and chemically comparable to the mineralized matrix of human bone. It is available in spongiosa (cancellous granules) and in blocks.

    Geistlich Bio-Oss® is the leading bone substitute for regenerative dentistry worldwide. The outstanding osteo-conductive properties of Geistlich Bio-Oss® lead to effective and predictable bone regeneration. Geistlich Bio-Oss® particles are incorporated over time within living bone which provides long-term volume preservation. The bio functionality of Geistlich Bio-Oss® is characterized by its topographic structure, hydrophilic properties and the biologic interaction that supports reliable bone formation.

    Leading clinicians rely on Geistlich Bio-Oss® because:

    • Geistlich Bio-Oss® augmented bone leads to high implant survival rates, comparable with implants placed in native bone.
    • Geistlich Bio-Oss® is easy to apply and can be used in a variety of therapeutic areas.
    • Geistlich Bio-Oss® is validated by 25 years of successful use and testing.
    • Geistlich Bio-Oss® is documented in more than 900 publications.

    Indications:

    • Augmentation or reconstructive treatment of the alveolar ridge; Filling of periodontal defects
    • Filling of defects after root resection, apicoectomy, and cystectomy
    • Filling of extraction sockets to enhance preservation of the alveolar ridge
    • Elevation of the maxillary sinus floor
    • Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)
    • Filling of peri-implant defects in conjunction with products intended for GBR

    Geistlich Bio-Oss® has excellent handling properties and provides predictable results in daily clinical use:

    • Before application, Geistlich Bio-Oss® is mixed with autogenous blood or a saline solution. Its hydrophilic properties promote rapid and complete hydration.
    • Geistlich Bio-Oss® is easily modelled and adheres optimally to the walls of the defect.
    • Excessive compression should be avoided in order to allow for new bone ingrowth.
    • Subsequent application of Geistlich Bio-Gide®, a collagen membrane, enables undisturbed healing which leads to new bone regeneration.

    Warnings:

    • Possible complications which may occur with any surgery include swelling at the surgical site, flap sloughing, bleeding, local inflammation, bone loss, infection or pain.
    • As Geistlich Bio-Oss Collagen® contains collagen, in very rare circumstances cases of allergic reactions may occur.

    Geistlich Bio-Oss® is available in eight convenient quantities of small or large granules, which adapt easily to defect sites:

    • Small Geistlich Bio-Oss® granules (0.25 – 1 mm) – available sizes: 0.25 g ~ 0.5 cc ; 0.5 g ~ 1 cc ; 1 g ~ 2 cc ; 2 g ~ 4 cc
    • Large Geistlich Bio-Oss® granules (1 – 2 mm) – available sizes: 0.5 g ~ 1.5 cc; 1 g ~ 3 cc; 2 g ~ 6 cc

    The package contains:

    • Geistlich Bio-Oss® 0.25-1mm, 0.5g=1cc

    Geistlich Bio-Gide® 25x25mm, 1 U/Bx

    Geistlich Bio-Gide® is the leading collagen membrane in North America for oral tissue regeneration. It is used in combination with a bone substitute such as Geistlich Bio-Oss® or Geistlich Bio-Oss Collagen®. Geistlich Bio-Gide® integrates with surrounding tissues to protect the initial coagulum. With its unique bilayer structure, Geistlich Bio-Gide® not only prevents ingrowth of soft tissue into the augmented site, but then optimally degrades to allow for the cascade of biologic events leading to regeneration.

    Geistlich Bio-Gide® is naturally resorbable therefore a second surgery for removal of the membrane is not required. As it simplifies the surgical technique, and exhibits excellent wound healing properties, Geistlich Bio-Gide® has fundamentally changed dental bone regeneration.

    Leading clinicians rely on Geistlich Bio-Gide® for:

    • Excellent tissue integration and undisturbed bone regeneration compared to using a bone substitute alone
    • Native collagen structure results in fewer dehiscences compared with other available membranes
    • Fully resorbable, no second surgery required for membrane removal
    • Predictable outcomes in the esthetic zone
    • Long-term data demonstrates predictable results in Guided Bone Regeneration (GBR) treatments when Geistlich Bio-Gide® is used in combination with Geistlich Bio-Oss®

    Indications:

    • Augmentation around implants placed in immediate and delayed extraction sockets
    • Localized ridge augmentation for later implantation
    • Alveolar ridge reconstruction for prosthetic treatment
    • Filling of bone defects after root resection, cystectomy, removal of retained teeth
    • GBR in dehiscence defects; and GTR procedures in periodontal defects

    Application of Geistlich Bio-Gide® is easy:

    • Measure the defect with a periodontal probe
    • Trim the dry collagen membrane to the desired shape and size
    • Apply dry with the rough side facing the defect
    • Moisten the membrane in situ with blood from the defect

    Geistlich Bio-Gide® is available in three convenient sizes:

    • 13 x 25 mm
    • 25 x 25 mm
    • 40 x 50 mm

    and a combination kit:

    • Geistlich Combi-Kit Collagen - Geistlich Bio-Gide® 16 x 22 mm with Geistlich Bio-Oss® 100 mg

    The package contains:

    • 1 membrane of Geistlich Bio-Gide® 25x25mm

    ANESTAject Plastic Hub 27G Short (25mm), 100 Needle/Bx

    These are HANSAmed’s exclusive brand of plastic hub needles: A pre-threaded, plastic hub needle that fits to your syringe as easily and securely as metal hub needles.

    Package contains:

    • 100 needles per box of Plastic Hub 27G Short (25mm)

    LIGHTHOUSE™ Physio Logic® Prof Deluxe Self-Taking Home Blood Press Kit, 1 U/Pk

    This easy-to-use, self-taking blood pressure kit is ideal for home use. Comes complete with vinyl zipper case, instruction booklet, and recording chart.

    The LIGHTHOUSE™ Medical Emergency Kit is designed to meet the basic medical emergency needs of a dental practice treating patients ranging from pediatric to geriatric. The goal of the LIGHTHOUSE™ Medical Emergency Kit is to equip dental clinics with the required medications to be complaint by today's standard. As an owner of a LIGHTHOUSE™ Medical Emergency Kit, you are automatically enrolled in a program called "Automatic Replenishment". The program is a service exclusively offered by HANSAmed to track, monitor and replenish each individual medication in your LIGHTHOUSE™ Medical Emergency Kit prior to expiration. This service guarantees your medications will remain current and up to date. The medications and devices included in a LIGHTHOUSE™ Kit are quick, safe and easy to administer.

    LighthouseTM provides dental clinics with vital medications, convenience, peace of mind and training to assist all dental staff in becoming equipped to handle a medical emergency in the office. With licensing and approval from Health Canada, we are able to provide clinics with quality medications to help you save a life.

    Features and benefits:

    • Latex-Free
    • Arm cuff size (measure upper arm circumference): 10 to 16 inches (25.4 to 40.6 cm)
    • Features a no-stop pin 300 mmHg gauge
    • Quality polyvinyl chloride (PVC) inflation system and calibrated nylon velcro cuff
    • Comes with a vinyl zippered case
    • Comes with instruction

    Package contains:

    • 1 unit of LIGHTHOUSE™ Physio Logic® Prof Deluxe Self-Taking Home Blood Press Kit

    Septodont Lignospan® standard Lidocaine HCl. 2% and Epi 1:100,000 Inj, USP, 50x1.7ml Carp/Bx

    Septodont Lignospan® contains 2% Lidocaine HCl injection with 1:100,000 epinephrine. When used for infiltration will have an average onset time of less than 2 minutes and a duration of about 60 minutes.

    Indications:

    • Local dental anesthesia by nerve block or infiltration

    Key Features:

    • No-methylparaben formulation to avoid allergic reactions on sensitive patients.
    • Lignospan when used for infiltration will have an average onset time of less than two minutes and a duration of about 60 minutes. When used for nerve blocks the average onset time is 2 to 4 minutes and will provide about 90 minutes of pulpal anesthesia.
    • 100 percent latex free components to help reduce allergic responses.
    • Terminal sterilization of product/cartridges for safe use.
    • Mylar label covered glass cartridges to minimize risk of wound in the event of a cartridge breakage.
    • Cartridges packed 10 to a blister tray to avoid glass to glass contact, hence reducing breakage.

    Presentation:

    • Box containing 5 blisters of 10 x 1.7ml glass cartridges

    Risk:

    • Reactions to Lignspan® are characteristic of those associated with other amide-type local anesthetics. A major cause of adverse reactions to this group of drugs is excessive plasma levels, which may be due to overdosage, inadvertent intravascular injection or slow metabolic degradation. Lignospan® is contraindicated in patients with a known hypersensitivity to it or to any local anesthetic agent of the amide type or to other components of lidocaine solutions. Local anesthetics should be employed only by clinicians who are well versed in diagnosis and management of dose-related toxicity and other acute emergencies which might arise from the block to be employed, and then only after insuring the immediate availability of oxygen, other resuscitative drugs, cardiopulmonary resuscitative equipment, and the personnel resources needed for proper management of toxic reactions and related emergencies. Lignospan® contains potassium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. Please see package insert for prescribing information.

    Package contains:

    • 50 cartridges – A box of 5 blisters of 10 x 1.7 ml glass cartridges
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